Umbralisib and Rituximab as Initial Therapy for Patients With Follicular Lymphoma and Marginal Zone Lymphoma

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Massachusetts General Hospital
Study ID
NCT03919175
Phase
PHASE2
Status
Terminated

Conditions

  • Follicular Lymphoma
  • Follicular Lymphoma Grade 2
  • Follicular Lymphoma Grade IIIa
  • Follicular Lymphoma, Grade 1
  • Lymphoma
  • Marginal Zone B Cell Lymphoma
  • Marginal Zone Lymphoma

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Umbralisib — DRUG
    Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
  • Rituximab — DRUG
    Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells

Study Details

This research is being done to assess Umbralisib and Rituximab as a first line therapy for Follicular Lymphoma or Marginal Zone Lymphoma.

Key Dates

Start date
Sep 1, 2019
Status verified
Feb 2026
Primary completion
May 5, 2024
Completion
May 5, 2024

Study Design

Enrollment
18 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Umbralisib+Rituximab
    * A treatment cycle is defined as 28 consecutive days. * Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24. * Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.

Primary Outcome Measure

Complete Response Rate [ Time Frame: 2 years ]

Locations (2)

FacilityCityStateZIPSite coordinators
Beth Israel Deaconness Medical CenterBostonMassachusetts02215-
Massachusetts General Hospital Cancer CenterBostonMassachusetts02114-

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